chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	261061195	261061196	T	C	34	GENIC	homozygous	108628945
1	261061343	261061344	A	G	38	GENIC	homozygous	108628946
1	261062309	261062310	C	T	31	GENIC	homozygous	108628947
1	261062511	261062512	T	A	52	GENIC	homozygous	108628948
1	261062607	261062608	C	T	50	GENIC	homozygous	108628949
1	261063147	261063148	C	T	45	GENIC	homozygous	108628950
1	261063350	261063351	C	A	45	GENIC	homozygous	108628951
1	261063577	261063578	T	C	24	GENIC	homozygous	108628952
1	261063904	261063905	C	T	43	GENIC	homozygous	108628953
1	261064049	261064050	G	C	39	GENIC	homozygous	108628954
1	261064841	261064842	T	A	51	GENIC	homozygous	108628955
1	261065122	261065123	A	T	33	GENIC	homozygous	108628956
1	261065917	261065918	T	C	35	GENIC	possibly homozygous	108628957
1	261066517	261066518	T	C	11	GENIC	homozygous	108628958
1	261068056	261068057	T	A	46	GENIC	homozygous	108628959
1	261068101	261068102	G	A	38	GENIC	homozygous	108628960
1	261068191	261068192	A	G	37	GENIC	homozygous	108628961
1	261068755	261068756	G	A	40	GENIC	homozygous	108628962
1	261069194	261069195	A	T	33	GENIC	homozygous	108628963
1	261069200	261069201	A	T	31	GENIC	homozygous	108628964
1	261069249	261069250	G	A	21	GENIC	possibly homozygous	108782584
1	261069916	261069917	A	C	34	GENIC	homozygous	108628965
1	261070246	261070247	T	C	42	GENIC	homozygous	108628966